HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 19780370, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Indanone | HCID 6735 | — |
| Reactant | [4-(Propan-2-yl)phenyl]hydrazine hydrochloride | HCID 2733248 | — |
| Reactant | Water ethanol | HCID 19096565 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19780370 | HCID 19780370 | — |
Reaction Steps
A mixture of 4-isopropylphenylhydrazine hydrochloride (6.3 g, 34 mmol) and 1-indanone (4.5 g, 34 mmol) were heated to reflux in ethanol (40 cm3) containing concentrated hydrochloric acid (2 cm3). Heating was continued for 4 hours, and then the reaction mixture was cooled to room temperature during which time the product crystallised out of solution as colourless crystals. This compound was filtered off, dried in a vacuum oven, and recrystallised from ethanol/water to yield colourless prisms. Yield: 6.59 g, (79%). M.p. 193° C. (from ethanol/water). 1H NMR (DMSO-d6) δ: 1.27 (6H, d,), 2.96 (1H, septet,), 3.65 (2H, s,), 6.9-7.6 (7H, m,), 11.2 (1H, br,).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05185360 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-faef046dc33b49c3b9aa721af3bced62 |
| Source note | uspto-grants-1993_02 |